Kyndt X, Reumaux D, Bridoux F, Tribout B, Bataille P, Hachulla E, Hatron P Y, Duthilleul P, Vanhille P
Department of Nephrology, Internal Medicine, Centre Hospitalier de Valenciennes, France.
Am J Med. 1999 May;106(5):527-33. doi: 10.1016/s0002-9343(99)00064-9.
To assess the value of serial determinations of antineutrophil cytoplasmic autoantibodies (ANCA) for monitoring disease activity in patients with systemic vasculitis.
Forty-three patients with histologically proven vasculitis (21 with Wegener's granulomatosis, 17 with microscopic polyangiitis, and 5 with renal-limited vasculitis) were studied for a median follow-up of 22 months. Disease activity was prospectively assessed and quantified by the Birmingham Vasculitis Activity Score. A total of 347 sera were analyzed for ANCA determination.
Relapses occurred in 23 (54%) of 43 patients. Diagnostic category (Wegener's granulomatosis vs micropolyangiitis and renal-limited vasculitis), severity of initial symptoms (mean vasculitis activity score, mean number of organs involved), and ANCA pattern [cytoplasmic-ANCA (c-ANCA) vs perinuclear-ANCA (p-ANCA)] did not significantly differ between relapsers and nonrelapsers. Lung involvement was more frequent at onset among relapsers [16 of 23 (70%) vs 6 of 20 (30%); P = 0.02]. Relapses were slightly, but not significantly, more frequent in patients with Wegener's granulomatosis or a c-ANCA pattern. The percentage of relapsers was greater in patients with persistently positive ANCA than in patients with negative or decreasing ANCA titers (86% vs 20%, P = 0.0001). However, the predictive value of an increase in ANCA titers for the occurrence of a subsequent relapse was only 28% (4 of 14) for c-ANCA, 12% (2 of 17) for anti-proteinase 3-ANCA, and 43% (6 of 14) for anti-myeloperoxidase-ANCA. An increase in ANCA occurred before or during relapse in 33% (10 of 30) of cases for c-ANCA/anti-proteinase 3 antibodies, and 73% (11 of 15) of cases for anti-myeloperoxidase antibodies.
The persistence of ANCA positivity is strongly associated with relapses. However, an increase in ANCA titers has a poor value for the early prediction of a subsequent relapse and should not be used as a sole parameter for therapeutic intervention. In addition, our results suggest that serial anti-myeloperoxidase determination may be useful as a prognostic marker in patients who are p-ANCA positive.
评估连续测定抗中性粒细胞胞浆自身抗体(ANCA)对监测系统性血管炎患者疾病活动度的价值。
对43例经组织学证实的血管炎患者(21例韦格纳肉芽肿、17例显微镜下多血管炎和5例局限于肾脏的血管炎)进行研究,中位随访时间为22个月。采用伯明翰血管炎活动评分对疾病活动度进行前瞻性评估和量化。共分析347份血清以测定ANCA。
43例患者中有23例(54%)复发。复发者与未复发者在诊断类别(韦格纳肉芽肿与显微镜下多血管炎及局限于肾脏的血管炎)、初始症状严重程度(平均血管炎活动评分、平均受累器官数量)及ANCA类型[胞浆型ANCA(c-ANCA)与核周型ANCA(p-ANCA)]方面无显著差异。复发者起病时肺部受累更为常见[23例中的16例(70%)对20例中的6例(30%);P = 0.02]。韦格纳肉芽肿或c-ANCA类型的患者复发略多,但无显著差异。ANCA持续阳性的患者复发率高于ANCA滴度阴性或下降的患者(86%对20%,P = 0.0001)。然而,ANCA滴度升高对随后复发的预测价值,c-ANCA为28%(14例中的4例),抗蛋白酶3-ANCA为12%(17例中的2例),抗髓过氧化物酶-ANCA为43%(14例中的6例)。c-ANCA/抗蛋白酶3抗体33%(30例中的10例)及抗髓过氧化物酶抗体73%(15例中的11例)在复发前或复发期间ANCA出现升高。
ANCA持续阳性与复发密切相关。然而,ANCA滴度升高对随后复发的早期预测价值不佳,不应作为治疗干预的唯一参数。此外,我们的结果提示,连续测定抗髓过氧化物酶可能对p-ANCA阳性患者作为预后标志物有用。